Daptomycin combinations as alternative therapies in experimental foreign-body infection caused by meticillin-susceptible Staphylococcus aureus

被引:9
作者
El Haj, Cristina [1 ]
Murillo, Oscar [1 ]
Ribera, Alba [1 ]
Vivas, Mireia [1 ]
Garcia-Somoza, Dolors [2 ]
Tubau, Fe [2 ,3 ]
Cabellos, Carmen [1 ]
Cabo, Javier [4 ]
Ariza, Javier [1 ]
机构
[1] Hosp Univ Bellvitge, IDIBELL, Infect Dis Serv, Lab Expt Infect, Barcelona 08907, Spain
[2] Hosp Univ Bellvitge, IDIBELL, Dept Microbiol, Barcelona 08907, Spain
[3] CIBERES ISCIII, Barcelona 08907, Spain
[4] Hosp Univ Bellvitge, IDIBELL, Dept Orthopaed Surg, Barcelona 08907, Spain
关键词
Foreign body infection; Combination therapy; MSSA; Daptomycin; EFFICACY; RIFAMPIN; RESISTANCE; LEVOFLOXACIN;
D O I
10.1016/j.ijantimicag.2015.04.004
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Whilst levofloxacin (LVX) in combination with rifampicin (RIF) is considered the optimal treatment for prosthetic joint infection (PJI) caused by meticillin-susceptible Staphylococcus aureus (MSSA), no therapeutic alternatives have been accurately evaluated. Based on the high effectiveness of the combination of daptomycin (DAP) plus RIF against meticillin-resistant S. aureus (MRSA) in this setting, in this study the efficacy of DAP+RIF and DAP+LVX combinations was tested as alternative therapies for foreign-body infections (FBIs) caused by MSSA. A tissue-cage infection model was performed using an MSSA strain. Male Wistar rats were treated for 7 days with LVX, DAP, RIF or the combinations LVX+RIF, DAP+RIF and DAP+LVX. Antibiotic efficacy was evaluated by bacterial counts from tissue cage fluid (TCF) and the cure rate was determined from adhered bacteria. Resistance was screened. Monotherapies were less effective than combinations (P<0.05), and resistance to DAP and RIF emerged. DAP+RIF (decrease in bacterial counts in TCF, 4.9 log CFU/mL; cure rate, 92%) was the most effective therapy (P<0.05). There were no differences between LVX+RIF (-3.4 log CFU/mL; 11%) and DAP+LVX (-3.3 log CFU/mL; 47%). No resistant strains appeared with combined therapies. In conclusion, the combinations DAP+RIF and DAP+LVX showed good efficacy and prevented resistance. DAP+RIF provided higher efficacy than LVX+RIF. These DAP combinations were efficacious alternatives therapies for MSSA FBI. Further studies should confirm whether DAP+RIF may be useful as a first-line therapy in the setting of PJI caused by MSSA. (C) 2015 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:189 / 195
页数:7
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